FSP CRA II (Zhengzhou)
Fortrea(1 month ago)
About this role
The role involves managing clinical site activities for trials in compliance with regulatory standards, overseeing monitoring responsibilities, and ensuring data integrity and participant safety. The position requires collaboration with study teams, preparation of monitoring plans, and participation in meetings related to clinical research projects.
Required Skills
- GCP
- ICH Guidelines
- Clinical Monitoring
- Regulatory Compliance
- Source Data Verification
- eTMF
- SAE Reporting
- Clinical Trials
- Data Management
- Medical Devices
About Fortrea
fortrea.comFortrea, a leading CRO, advancing clinical trials through patient-focused clinical solutions that accelerate clinical development, drive trial success, and bring innovative therapies to those who need them most.
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